| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71809024-71809120 | Rare:39 | ||||
| chr16:71845874-71846029 | Common:2; Rare:55 | ||||
| chr16:71895250-71895584 | Common:3; Rare:129 | ||||
| chr16:72093565-72093964 | Rare:98 | ||||
| chr16:74296462-74296987 | Common:1; Rare:175 | ||||
| chr16:74304039-74304393 | Common:2; Rare:78 | ||||
| chr16:74701140-74701343 | Common:1; Rare:47 | ||||
| chr16:75433339-75433852 | Common:4; Rare:169 | ||||
| chr16:75464372-75464483 | Common:2; Rare:55 | ||||
| chr16:75623229-75623370 | Common:3; Rare:48 | ||||
| chr16:75647614-75647837 | Common:2; Rare:111; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648220-75648356 | Rare:45 | ||||
| chr16:75648636-75648666 | Rare:14 | ||||
| chr16:77190596-77191010 | Common:14; Rare:142 | ||||
| chr16:77191102-77191231 | Common:2; Rare:53 |